Canonical Allele Identifier: PA916073958
Gene: SEC23B HGNC NCBI

Linked Data

ClinVar Variation Id: 663227
ClinVar RCV Id: RCV000821067 RCV003141852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116781.1:p.Thr297Ile
CA408360134
NM_032986.5:c.890C>T